GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gluD in Halomonas xinjiangensis TRM 0175

Align GluD aka CGL1953, component of Glutamate porter (characterized)
to candidate WP_043531024.1 JH15_RS12965 amino acid ABC transporter permease

Query= TCDB::P48245
         (273 letters)



>NCBI__GCF_000759345.1:WP_043531024.1
          Length = 396

 Score = 65.9 bits (159), Expect = 1e-15
 Identities = 50/170 (29%), Positives = 83/170 (48%), Gaps = 5/170 (2%)

Query: 48  GTALGLGRISEIRILRWFCAVIIETFRAIPVLILMIFAYQMFAQYNIVPSSQLAFAAVVF 107
           G  L  G IS   IL     V++ T   +   +  +  +       ++P     F A+  
Sbjct: 214 GKRLPAGWISLALILGLPLLVLLVTGVPVTWDVPALSGFNFRGGITVIPE----FLALWL 269

Query: 108 GLTMYNGSVIAEILRSGIASLPKGQKEAAIALGMSSRQTTWSILLPQAVAAMLPALISQM 167
            L++Y  S IAEI+RSGI ++  GQ EAA AL +        +++PQA+  ++P L SQ 
Sbjct: 270 ALSIYTASFIAEIVRSGIQAISHGQTEAAQALSLPQGLILRLVIVPQAMRVIIPPLTSQY 329

Query: 168 VIALKDSALGYQIGYIEVVRSGIQSASVNRNYLAALFVVALIMIVLNFSL 217
           +  +K+S+L   IGY ++V S     ++N+   A   +   + + L  SL
Sbjct: 330 LNLIKNSSLATAIGYPDLV-SVFAGTTLNQTGQAIEVIAMTMAVYLTISL 378



 Score = 41.6 bits (96), Expect = 3e-08
 Identities = 38/138 (27%), Positives = 62/138 (44%), Gaps = 8/138 (5%)

Query: 27  LPGLWGTLKSAVFSVILALVMGTALGLGRISEIRILRWFCAVIIETFRAIPVLILMIFAY 86
           L GL  TL  +   V+ A ++G  +G+ R+S   ++       IE FR IP+L+ + F Y
Sbjct: 88  LVGLLNTLIVSALGVLAATIIGFVVGIARLSPNWLIARLATCYIEIFRNIPLLLQIFFWY 147

Query: 87  QMFAQYNIVPSSQ--LAFAAVVFGLTMYNGSVIAEILRSGIASLPKGQKEAAIALGMSSR 144
             FA    +PS++  ++   V+F L +    +      SG   +P       IA+  S  
Sbjct: 148 --FAVLRTMPSARESMSLGEVIF-LNVRGLYLPEPQFLSGFGLIPAA---FVIAVVASIA 201

Query: 145 QTTWSILLPQAVAAMLPA 162
              W+    +A    LPA
Sbjct: 202 FALWNKRRQEATGKRLPA 219


Lambda     K      H
   0.323    0.136    0.395 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 259
Number of extensions: 15
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 273
Length of database: 396
Length adjustment: 28
Effective length of query: 245
Effective length of database: 368
Effective search space:    90160
Effective search space used:    90160
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory